Primary Site >> Stomach Cancer
Gene >> ADGRF5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265417 |
| Start | 46878261:46878261(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1181A>G |
| AA Mutation | p.Gln394Arg(p.Q394R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265417 |
| Start | 46884176:46884176(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138516675 |
| CDS Mutation | c.424C>T |
| AA Mutation | p.Arg142Cys(p.R142C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265417 |
| Start | 46863070:46863070(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201326559 |
| CDS Mutation | c.2017G>A |
| AA Mutation | p.Val673Ile(p.V673I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265417 |
| Start | 46906698:46906698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780842238 |
| CDS Mutation | c.65C>T |
| AA Mutation | p.Ala22Val(p.A22V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265417 |
| Start | 46854063:46854063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3970A>C |
| AA Mutation | p.Asn1324His(p.N1324H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265417 |
| Start | 46856024:46856024(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3911C>T |
| AA Mutation | p.Ser1304Phe(p.S1304F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265417 |
| Start | 46859465:46859465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2438T>G |
| AA Mutation | p.Val813Gly(p.V813G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265417 |
| Start | 46884170:46884170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768297112 |
| CDS Mutation | c.430G>A |
| AA Mutation | p.Val144Ile(p.V144I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265417 |
| Start | 46859033:46859033(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2870G>T |
| AA Mutation | p.Trp957Leu(p.W957L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265417 |
| Start | 46858605:46858605(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754646677 |
| CDS Mutation | c.3298G>A |
| AA Mutation | p.Val1100Ile(p.V1100I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265417 |
| Start | 46858215:46858215(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3688C>A |
| AA Mutation | p.Leu1230Ile(p.L1230I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265417 |
| Start | 46858815:46858815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3088T>C |
| AA Mutation | p.Cys1030Arg(p.C1030R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265417 |
| Start | 46858433:46858433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141322343 |
| CDS Mutation | c.3470C>T |
| AA Mutation | p.Thr1157Met(p.T1157M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265417 |
| Start | 46860819:46860819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2275G>A |
| AA Mutation | p.Ala759Thr(p.A759T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265417 |
| Start | 46863014:46863014(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201435302 |
| CDS Mutation | c.2073C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265417 |
| Start | 46860811:46860811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2283T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265417 |
| Start | 46858216:46858216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750705875 |
| CDS Mutation | c.3687C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265417 |
| Start | 46882093:46882093(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140241968 |
| CDS Mutation | c.627C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |